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The GLP1R transactivation assay was established in our lab and reported previously45,46,47.
A fast and reliable Multiplex-PCR assay was established to identify the species Lactobacillus johnsonii.
A cell culture assay was established for the determination of bioactivity of released IL-18.
Thereby, a novel highly sensitive fluorescence strategy for silver(I) assay was established.
A mammalian cell reporter assay was established, using de novo mutations at the human AAVS1 locus as a readout of Cas9 nuclease activity.
Using ∼1 mg of VRC01-WT mAb per assay, the precision of the micro-PEG assay was established.
To study the bone targeting potential of these conjugates, an in vitro HAP binding assay was established.
The mRT-PCR assay was established successfully for the detection and differentiation of avian H3, H5, and H9 subtype AIVs and NDVs.
Nested PCR assay was established based on primers design and applied to seven fecal samples from road killed birds containing nematode and/or trematode eggs.
In order to detect this new emerging virus rapidly and reliably, a TaqMan-based real-time RT-PCR assay was established in this study.
Further, the sensitivity of the assay was established to be 0.1% for the detection of adulteration, while limit of detection of ovine DNA was as low as 1 pg.
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